ENST00000261609.13:c.11724A>G
MANE Select
|
ENSP00000261609.8:p.Leu3908=
|
|
ENST00000650509.1:c.3435A>G
|
ENSP00000496936.1:p.Leu1145=
|
|
ENST00000261609.11:c.11724A>G
|
ENSP00000261609.7:p.Leu3908=
|
|
ENST00000564519.1:n.239A>G
|
|
|
NM_004667.5:c.11724A>G
|
NP_004658.3:p.Leu3908=
|
|
XM_005268276.3:c.11610A>G
|
XP_005268333.1:p.Leu3870=
|
|
XM_005268277.3:c.11610A>G
|
XP_005268334.1:p.Leu3870=
|
|
XM_006720726.2:c.11709A>G
|
XP_006720789.1:p.Leu3903=
|
|
XM_006720727.2:c.11466A>G
|
XP_006720790.1:p.Leu3822=
|
|
XM_011522131.1:c.11241A>G
|
XP_011520433.1:p.Leu3747=
|
|
XM_011522132.1:c.9240A>G
|
XP_011520434.1:p.Leu3080=
|
|
XM_011522133.1:c.8469A>G
|
XP_011520435.1:p.Leu2823=
|
|
XM_011522134.1:c.5841A>G
|
XP_011520436.1:p.Leu1947=
|
|
XM_005268276.5:c.11610A>G
|
XP_005268333.1:p.Leu3870=
|
|
XM_006720726.3:c.11709A>G
|
XP_006720789.1:p.Leu3903=
|
|
XM_006720727.3:c.11466A>G
|
XP_006720790.1:p.Leu3822=
|
|
XM_017022695.1:c.11610A>G
|
XP_016878184.1:p.Leu3870=
|
|
XM_017022696.1:c.11610A>G
|
XP_016878185.1:p.Leu3870=
|
|
XM_017022697.1:c.4890A>G
|
XP_016878186.1:p.Leu1630=
|
|
XM_017022698.1:c.4890A>G
|
XP_016878187.1:p.Leu1630=
|
|
NM_004667.6:c.11724A>G
MANE Select
|
NP_004658.3:p.Leu3908=
|
|